# FDA Inspection 1110941 - Intermedic Arfran S.A. - November 14, 2019

Source: https://www.keypedia.com/records/fda_inspections/intermedic-arfran-sa/b6f1f2cc-6761-4fa7-a7c6-1bdf7927ca80
Source feed: FDA_Inspections

> FDA Inspection 1110941 for Intermedic Arfran S.A. on November 14, 2019. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1110941
- Company Name: Intermedic Arfran S.A.
- Inspection Date: 2019-11-14
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1110941 - 2019-11-14](https://www.keypedia.com/records/fda_inspections/intermedic-arfran-sa/5750c90a-81d9-4f17-b9be-87a722c0569d)
- [FDA Inspection 958881 - 2016-02-05](https://www.keypedia.com/records/fda_inspections/intermedic-arfran-sa/c6d9eea3-c219-4081-ba1a-b5b5a0314d72)
- [FDA Inspection 958881 - 2016-02-05](https://www.keypedia.com/records/fda_inspections/intermedic-arfran-sa/d6f4093a-2562-41f9-b3db-4ab6ade2480d)

Company: https://www.keypedia.com/companies/intermedic-arfran-sa/ff91ad41-f31f-4e03-b74b-beb6ca629004

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7